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Physical Activity clinical trials

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NCT ID: NCT01669564 Completed - Quality of Life Clinical Trials

Functional Assessment Screening Patient Reported Information

FAST-PRI
Start date: February 2013
Phase: N/A
Study type: Interventional

This study will evaluate a new tool, based on our currently implemented "Functional Assessment Screening Tablets (FAST)," and activate patients to partner with their physicians. Completion of this project, FAST-PRI, will provide important information on the effectiveness of using HIT patient feedback to inform and activate patients and promote health behavior change. Aim 1 Hypotheses: Patients who receive self-management support through HIT patient feedback (intervention) will be more likely than patients who do not receive such feedback (control) to: - Initiate discussions with their provider regarding study-designated PRI; - Have discussions with their providers, regardless of the initiator, regarding study-designated PRI; and - Perceive these discussions of study-designated PRI to be useful. Approach: We will conduct a 12-month randomized controlled trial of HIT patient feedback, clustered at the physician level, in an academic group medical practice. Patients and providers will complete questionnaires regarding discussions of health behaviors and HRQoL at each clinical encounter. Aim 2 Hypotheses: HIT patient feedback will result in: 1) increased number of smoking quit attempts, 2) increased physical activity, and 3) improved mental HRQoL at six, and twelve months. Approach: Patient participants will complete questionnaires regarding smoking quit attempts, physical activity, and their mental HRQoL at baseline, six and twelve months. Aim 3 Hypotheses: For each study-designated PRI, patients who receive HIT patient feedback will: 1) receive more treatment recommendations (e.g., nurse educator, pharmacist, social worker referrals); 2) act on more treatment recommendations; and 3) exhibit improved self-efficacy regarding their ability to make positive lifestyle changes and improve their HRQoL; physicians whose patients receive HIT patient feedback will have higher self-efficacy regarding their ability to influence their patients to make positive lifestyle changes and improve HRQoL. These, in addition to discussions (Aim 1), will mediate the relationship between HIT patient feedback and improvements in study-designated PRI. Approach: We will survey patients and physicians and abstract referral data from the electronic medical record (EMR).

NCT ID: NCT01664585 Completed - Quality of Life Clinical Trials

Exercise Training With Physically Active Lifestyle to Reduce Headache and Quality of Life

HEADEX
Start date: September 17, 2012
Phase: N/A
Study type: Interventional

The aim of this intervention study is to examine whether tailored exercise therapy training is effective and cost-effective to decrease headache frequency and intensity, reduce medication used for chronic headache and patients´ absence from work, improve their neck muscle force, cervical spine mobility, functional ability and quality of life, and increase general physical activity in chronic headache women at regular work during a 6-month intervention. The intervention itself with pilot-tested upper-neck specific exercise regimen aims that patients would independently commit to train and exercise to reduce their headache, and thus increase their quality of life. In addition, reduced pain and frequency of headache may increase the objectively measured daily physical activity of chronic headache patients.

NCT ID: NCT01657422 Completed - Physical Activity Clinical Trials

PACE+: Counseling Adolescents for Exercise and Nutrition

PACEAdol
Start date: August 2000
Phase: N/A
Study type: Interventional

PACE+ was developed to address the increased number of adolescents in our country that are at risk for cardiovascular disease, cancer, and other diseases due to inactivity, obesity, and malnourishment. PACE+ will evaluate the efficacy of an integrated clinical and home-based intervention to improve physical activity and nutrition behaviors in adolescents ages 11-15 over a period of 2 years. This study is unique in that it will be one of the first to evaluate a combined physical activity and nutrition intervention for youth that revolves around the primary health care setting. The PACE+ intervention is particularly innovative in that three components - computer, provider counseling, and an extended home-based intervention - are unified through a common theoretical framework.

NCT ID: NCT01643538 Completed - Physical Activity Clinical Trials

Social Goals and Individual Incentives to Promote Walking in Older Adults

Start date: August 2012
Phase: N/A
Study type: Interventional

The goal of this randomized and controlled trial is to test whether a financial incentive of a donation to achieve a social goal is more effective to motivate and sustain a daily walking habit than the same dollar value given to an older adult. The investigators will achieve this using a novel computer platform utilizing a digital pedometer-internet interface.

NCT ID: NCT01633918 Completed - Physical Activity Clinical Trials

FeetEnergy Approach to Increase Physical Activity and Reduce Screen Time in Adolescents

FeetEnergy
Start date: August 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to find out whether an Internet-supported FeetEnergy approach and two home works integrated in three health education lessons can increase adolescents' active commuting to school and leisure-time physical activity and decrease their screen time.

NCT ID: NCT01626807 Completed - Obesity Clinical Trials

Evaluation of a Walking School Bus Program

Start date: December 2012
Phase: N/A
Study type: Interventional

Just two generations ago, walking or bicycling to school was the norm for a substantial number of US children, e.g. 48% of children walked or biked to school in 1969 versus only 13% in 2009. This decline occurred in the same timeframe as the childhood obesity epidemic, which is at record high levels in the US and affects low-income and ethnic minority children the most. This project will test "the walking school bus" (WSB) program, in which children walk to and from school with adults, and its impact on low-income, ethnic minority children's walking to school, physical activity, and risk for obesity. Ultimately, this line of research has the potential to provide a low-cost, easy to disseminate program to reduce risk of obesity and cancer for at-risk children. The investigators Specific Aims among 3rd-5th grade children include: SA1) To recruit 770 child-parent dyads from 22 elementary schools over 4 years and conduct a cluster randomized controlled trial to assess the efficacy of a WSB program on children's walking to school, physical activity, and BMI z-score over a school-year SA2) To collect and analyze data on individual-, school-, and macro-level influences on changes to children's walking to school resulting from the WSB program The Primary Hypotheses to be tested, in comparison to control children, include: H1) The WSB program will increase children's walking to school over a school-year. H1a) Parents' outcome expectations and self-efficacy will mediate the relationship between the WSB and changes to children's walking to school. H1b) Walkability, safety, and acculturation will moderate changes to children's walking to school. H2) The WSB program will increase children's physical activity and decrease BMI z-scores over a school-year. H3) The WSB program will increase school-level pedestrian safety behaviors over a school-year.

NCT ID: NCT01621035 Completed - Physical Activity Clinical Trials

Objective Assessment of Physical Activity in Older Adults

Start date: November 2011
Phase: N/A
Study type: Observational

The purpose of the present study is to evaluate the validity of 2 objective measures of physical activity among older adults. In addition, the investigators will examine the influence of functionality, walking aids, walking speed and step length on the accuracy.

NCT ID: NCT01610323 Completed - Obesity Clinical Trials

Fitness Improvement in Obese, Pregnant Women: an Intervention Trial

InterGOFIT
Start date: October 2011
Phase: N/A
Study type: Interventional

In pregnancy, the adoption or pursuit of a sedentary lifestyle contributes to the development of co-morbid conditions such as hypertension, maternal and childhood obesity, gestational diabetes, pre-eclampsia, cesarean section and delivery of large-for-gestational-age infants (LGA). The aim of this study is to test the hypothesis that obese, pregnant women following a supervised moderate intensity physical conditioning program during the 2nd trimester of pregnancy will maintain a higher level of physical activity up to the end of pregnancy, as compared to women in the control group. We will also conduct a pilot study on the feasibility to examine the effects of the intervention on maternal fitness and neonatal anthropometry.

NCT ID: NCT01588392 Completed - Physical Activity Clinical Trials

Short bouTs of Exercise for Preschool-age Children

STEP
Start date: November 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to examine if short bouts of structured physical activity implemented within the classroom setting as part of designated gross-motor playtime will increase preschool-age children during-school physical activity level.

NCT ID: NCT01588379 Completed - Physical Activity Clinical Trials

Mothers and Girls Dancing Together Trial

MAGNET
Start date: January 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the feasibility and efficacy of a 12-week afterschool afro-centric dance physical activity program for daughters and mothers on the physical activity level of African-American girls.